FDA inspection
Guidewire Technologies, Inc.: FDA inspection ending Apr 21, 2006
FDA inspection 424967 · Voluntary Action Indicated (VAI) · Salem, NH
Key facts
| Inspection ID | 424967 |
|---|---|
| Firm | Guidewire Technologies, Inc. |
| FEI number | 1221806 |
| Address | 26 Keewaydin Dr |
| City | Salem |
| State | NH |
| ZIP | 03079-4853 |
| Fiscal year | 2006 |
| Inspection end date | Apr 21, 2006 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data